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FDA 510(k)

ALTRA PRESS-FIT HIP SYSTEM

K-Number: K063002 · 2006-10-31

Decision Date2006-10-31
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALTRA PRESS-FIT HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2006-10-31 under 510(k) number K063002. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTRA PRESS-FIT HIP SYSTEM?

ALTRA PRESS-FIT HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-31. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K063002.

When did ALTRA PRESS-FIT HIP SYSTEM receive FDA 510(k) clearance?

ALTRA PRESS-FIT HIP SYSTEM received FDA 510(k) clearance on 2006-10-31, under 510(k) number K063002.

Who is the listed applicant for ALTRA PRESS-FIT HIP SYSTEM?

The FDA 510(k) record lists Biomet Manufacturing Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALTRA PRESS-FIT HIP SYSTEM?

The FDA product code for ALTRA PRESS-FIT HIP SYSTEM is KWA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Biomet Manufacturing Corp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KWA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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